research associate

The Association For Manufacturing Technology

<div>Description:

About the team:
AMT&rsquo;s Research Services team is responsible for planning, producing, and delivering market research and industry benchmarking surveys to customers ranging from high-growth startups to multinational corporations. With a foundation in economics as well as a wide range of manufacturing technologies, the team provides insight across diverse areas of the industry. You&rsquo;ll be surrounded by a growing Research Services team based in McLean, VA with backgrounds as diverse as hard tech, investment banking, economics, mathematics, data science, consulting, and political science. The strategic analytics team collaborates with DevOps, content, marketing, membership, sales, exhibitions, advocacy, and global services teams to grow AMT&rsquo;s customer base, industry engagement, and thought leadership.
About the role:
Research associates are immersed in AMT&rsquo;s proprietary market research products alongside independent sources to support hundreds of the top companies in the industry. This role involves creating compelling market research data and analysis in order to deliver insights to industry leaders looking to make strategic decisions with confidence. AMT research associates grow to become interdisciplinary experts across a combination of technology, business, finance, and entrepreneurship topics. As part of that growth, associates accelerate their development by regularly attending and participating in trade shows and conferences, as well as interacting with clients on a regular basis.
Responsibilities<ul><li>Conduct research using a wide range of sources, including business and trade press, market reports, interviews, conference presentations, surveys, academic publications, and patent filings</li><li>Build relationships with AMT&rsquo;s market research subscribers and the broader industry</li><li>Produce and present market research to subscribers</li><li>Attend and, in some cases, participate in trade shows and other industry events as an AMT representative</li><li>Collaborate internally to prioritize market research tasks, subscriber needs, and associate development</li><li>This position is an in-office role and requires between 5% and 15% travel annually</li></ul>
Requirements:
<ul><li>Bachelor's degree in science, engineering, mathematics, or economics discipline (required); relevant graduate degrees helpful</li><li>No prior years of work experience required; Applicants with years of experience commensurate with Senior Research Associate and Associate roles are encouraged to apply</li><li>Strong listening, writing, and speaking abilities, as well as attention to detail and organization; writing ability includes coverage of business and technical topics</li><li>The role requires a collaborative approach within the research team, where success is defined by meeting client needs as a group, which includes significant client-facing interactions in a consulting capacity</li><li>Prior market research experience of any kind preferred</li><li>Prior experience with product design, development, or manufacturing processes strongly preferred</li><li>Prior experience in developing data processes, automating data processes, and/or building business intelligence applications helpful</li><li>Proficient in using Microsoft Word, Excel, PowerPoint, and Outlook. SQL and experience with business analytics and data visualization packages (PowerBI, Tableau or similar) is preferred. Proficiency or familiarity with using statistical tools is helpful but not required.</li></ul>
Full-Time Benefits:<ul><li>Medical | Dental | Vision coverage &ndash; 100% of premiums covered for employees and eligible dependents</li><li>Paid Time Off (PTO) &ndash; up to 5 weeks if start date is before July 1. After July 1, receive 2.5 weeks for the remainder of the year.</li><li>Paid Winter Break and select holidays</li><li>Tuition reimbursement program</li><li>401k Plan (100% company match up to 6%, no vesting period)</li><li>Free drinks/snacks/lunch catered monthly and so much more&hellip;.</li></ul>
Equal Opportunity Employer:
AMT is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, race, color, sex, religion, national origin, disability, sexual orientation, gender identity or expression, pregnancy status, marital
status, military or veteran status, genetic disposition, or any other reason protected by law.</div>

Research Associate

American Regent

<div>Nature and Scope 
The Research associate is responsible for performing analytical activities to provide support for formulation development and process development.<div>
Essential Duties and Responsibilities 
Nothing in this job description restricts management&rsquo;s right to assign or reassign duties and responsibilities to this job at any time. 
<ul><li>Develop methods for raw materials, in-process and finished drug product under cGLP/cGMP, ICH, USP/EP Guideline.</li><li>Perform sample testing using HPLC, UPLC, UV/VIS, GC, particle sizer, pH meter, etc. to provide support for formulation and process development.</li><li>Conduct analytical studies in support of formulation development, process development, process scale-up, and stability studies.</li><li>Develop, modify, and optimize SOPs and test methods as appropriate.</li><li>Conduct literature search for method development.</li><li>Organize and prepare samples for analysis by external laboratories.</li><li>Troubleshoot and maintain analytical equipment.</li><li>Observe and maintain compliance, safety regulations, cGLP/GMP guidelines, and company policies and procedures.</li><li>Perform any other tasks/duties as assigned by management.</li></ul></div><div>
Education Requirements and Qualifications 
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. 
<ul><li>BS degree in pharmaceutical science, chemistry, biology, or life science related field.</li><li>Method development experience in the pharmaceutical industry, preferred.</li><li>Prior experience in pharmaceutical, analytical, or research laboratory settings preferred.</li><li>Ability to work independently and collaboratively in a fast-paced laboratory environment.</li></ul></div><div> 
 Physical Environment and Requirements 
<ul><li>Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees.</li><li>Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision.</li><li>The employee is required to safely handle, use, and dispose of chemicals.</li><li>Able to lift and/or move up to 50 pounds and stand on feet for approximately 4-8 hours.</li></ul></div> 
Expected Salary Range:
$70,100-$75,000
The salary range displayed is the minimum and maximum annual salary range of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate&rsquo;s qualifications, education, knowledge, skills and experience.
American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a wide
range of other benefits.
American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.
Applicants have rights under Federal Employment Laws.
<ul><li>FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf</li><li>
Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)</li><li>
Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf</li></ul>
Alert: We&rsquo;re aware of individuals impersonating our staff to target job seekers. Please note:<ul><li> All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.</li><li> Our recruiting process includes multiple in person and/or video interviews and assessments.</li><li> If you are unsure about the legitimacy of a message, contact John Rossini at jrossini@americanregent.com before responding.</li><li> We never request payment, bank information, or personal financial details during our offer process.</li></ul>
Your security is important to us, and we encourage you to stay vigilant when job searching.
American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email hrtalentacquisition@americanregent.com.</div>

The University of Iowa

Posting ID 159983
 Department Periodontics/College of Dentistry
 Jobcode Temp Employee - Non-UI Student
 Working Title Laboratory Research Associate
 Details
 
Dr. Ganesan’s lab in the Department of Periodontics is seeking an Undergrad Research Associate. The lab focuses on basic, clinical translational projects and clinical trials investigating oral microbiome-host interactions in periodontal health and disease in specific patient populations.
 
Specific duties will include: 
<ul>
<li>-Providing laboratory assistance including solution preparation</li>
<li>-Equipment cleaning, washing and maintenance</li>
<li>-Monitoring tests and experiments in a supervised academic research setting</li>
<li>-Cataloging, and cleaning field equipment, and data entry</li>
<li>-Assisting with some general laboratory tasks.</li>
<li>-Prepare media and solutions</li>
<li>-Extract genomic and plasmid DNA, and RNA</li>
<li>-Working with the primary epithelial cell culture from patients with and without obesity</li>
<li>-Performing PCR, Western blot, fluorescent microscopy and culturing microorganisms</li>
<li>-Collecting and analyzing data and be responsible for keeping a laboratory notebook</li>
<li>-Will be responsible for preparing and autoclaving standard laboratory solutions and media</li>
</ul>
Desirable qualifications: 
<ul>
<li>-Demonstrated knowledge in human anatomy, chemistry, biology</li>
<li>-Pre-dental degree major</li>
<li>-Demonstrated ability to work in a team setting</li>
<li>-Demonstrated communication skills</li>
</ul>
Work schedule: M-F, between hours of 8:00am – 5:00pm. As close to 18-20 hours / week as possible, flexible.
 
Rate of Pay: $11.00/Hour
 
Contact ROBERT BELAND
 Email: robert-beland @uiowa.edu
 Application Instructions Please send a resume to Rob Beland at the above email.
 Ad Start Date 06/22/2026
 Ad End Date 06/25/2026

Laboratory Research Associate

Alliance for Clinical Trials in Oncology

<div>
 
 The Alliance for Clinical Trials in Oncology Foundation (Foundation) is a foundation created to enhance and expand the ability of the Alliance for Clinical Trials in Oncology (Alliance) to conduct cancer clinical research and address important treatment questions through large-scale clinical trials. Through efforts of the Foundation in support of the Alliance, clinical trials and laboratory research are conducted to discover new or improved ways to prevent, treat, and cure many types of cancer, including leukemia and lymphoma, and cancers of the breast, prostate, lung, and gastrointestinal (GI) tract, and help educate the medical community on methods of cancer diagnosis, treatment, and prevention.
 
 
 In May 2014, the Foundation created the Alliance Foundation Trials, LLC (AFT), respectively, a wholly-owned subsidiary of the Foundation. AFT was also created to conduct cancer clinical research and address medical care and treatment through large-scale clinical trials involving various industry-related partners.
 
 
 The Alliance Foundation Trials (AFT) is seeking a Clinical Research Associate (CRA) to support the management and execution of clinical trial operations across AFT studies. This role is responsible for key site management and study start-up activities, including feasibility assessments, site selection support, maintenance of trial master files (eTMF), and oversight of clinical trial systems such as CTMS. The CRA will collaborate closely with CROs, vendors, and investigative sites to ensure studies are conducted in compliance with ICH GCP guidelines and organizational standards, while supporting studies from start-up through ongoing maintenance. Come join an organization full of passionate, team-oriented professionals driven to change the face of cancer.
 
 
 Benefits of working at the Alliance for Clinical Trials in Oncology Foundation{{:}}
 
 <ul>
 <li>
 8 weeks of paid time off (including PTO, sick, and holidays) during year one
 </li>
 <li>
 Medical, Dental &amp; Vision plans with a 100% employer-paid option for employees
 </li>
 <li>
 Tuition reimbursement stipends
 </li>
 <li>
 Continuing Education
 </li>
 <li>
 3% employer match for retirement investments
 </li>
 <li>
 Annual Employee Performance Bonus Program
 </li>
 <li>
 Annual Cost of Living Adjustment
 </li>
 <li>
 50% commuter reimbursement
 </li>
 <li>
 Healthy Work/Life balance and flexibility
 
 </li>
 </ul>
 
 
 ROLE AND RESPONSIBILITIES
 
 
 
 &bull; Assist operations team in supporting the Alliance member sites and escalate site related issues when necessary.
 
 
 &bull; Send, track, and review study-specific and global feasibility questionnaires.
 
 
 &bull; Assist with site selection and recruitment by generating site identification reports (e.g., site accrual); collecting, reviewing and tracking site feasibility/credentialing documentation and follow-up on site accruals accordingly.
 
 
 &bull; Track training information and issue trainings for sites and contacts.
 
 
 &bull; Collection of essential documents related to study start-up and review IP release packages.
 
 
 &bull; Prepare for and execute Investigator meetings and other site training programs.
 
 
 &bull; Assist with creation of start-up plans and templates.
 
 
 &bull; Ensure proper and timely filing of all relevant study documents into the eTMF on an ongoing basis to ensure compliance with applicable work instructions, SOPs and ICH GCP guidelines and AFT expectations.
 
 
 &bull; Perform routine review of filing procedures to ensure adherence to current quality guidelines at all times.
 
 
 &bull; Accurately enter and manage data within the Clinical Trial Management System (CTMS) by{{:}} tracking completed training information that could carry over to other studies; maintaining site information and rosters; reviewing monitoring reports to identify deficiencies, reviewing adequacy of issue escalation and issue resolution; and provide feedback to appropriate CRO contacts.
 
 
 &bull; Participate in co-monitoring activities.
 
 
 &bull; Communicate with CROs, vendors, and/or study sites as necessary to support the study, which includes monitoring email accounts related to studies.
 
 
 &bull; Conduct regulatory review of ICF changes and coordinate review by Executive Officer and contracts team
 
 
 &bull; Coordinate study related meetings; take detailed minutes at meetings on decisions and action items and distribute to the team, as assigned.
 
 
 &bull; Other related duties as assigned to meet departmental and company objectives.
 
 
 
 
 Requirements
 
 
 
 
 
 QUALIFICATIONS AND EDUCATION REQUIREMENTS
 
 
 
 &bull; A minimum of a BA/BS degree is required.
 
 
 &bull; Degree in a health or science major preferred.
 
 
 &bull; 2 - 4 years relevant experience in biotech, pharma, and/or CRO, including 1 year of clinical research industry experience.
 
 
 &bull; Working knowledge of clinical monitoring responsibilities and procedures.
 
 
 &bull; Previous experience with eTMF, CTMS, and IRT clinical trial systems is strongly preferred.
 
 
 &bull; Proficient in Microsoft Office Suite, especially Word and Excel.
 
 
 
 PREFERRED SKILLS
 
 
 
 &bull; Strong organizational skills and ability to prioritize workload to meet tight deadlines in a fast-paced and dynamic work environment.
 
 
 &bull; Strong interpersonal, written, and verbal communication skills.
 
 
 &bull; Flexible and adaptable to a small business workplace environment.
 
</div>

Clinical Research Associate

City of Hope

<div><div>Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
City of Hope has a Clinical Research Associate II (CRA II) opportunity available. The CRA II manages an assigned set of multiple research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed.
As a successful candidate, you will:<ul><li>
Conduct protocol management for an assigned set of multiple research protocols.</li><li>
Maintain current and accurate protocol documentation; notify investigators of pertinent protocol changes.</li><li>
Ensure that patients are appropriately registered; maintain documentation of patient registration.</li><li>
Compile and submits data on appropriate forms according to protocol requirements.</li><li>
Ensure protocol compliance with intense monitoring of specific study requirements and schedules protocol related treatment and tests.</li><li>
Plays active role in recruitment of patients to study.</li><li>
Train and mentor new clinical research staff members.</li><li>
Collect and deliver specimens for analysis, using appropriate or specified equipment for collecting and handling specimens.</li><li>
Works with physician or nurse to see that protocol related tests and evaluations are ordered per protocol guidelines.</li></ul></div><div>
Your qualifications should include:<ul><li>
Associate&rsquo;s degree.</li><li>
Experience may substitute for minimum education requirements.</li><li>
One year of experience working in a health care setting, preferably in research.</li><li>
Must have a minimum of 6 months experience/training as a CRA I at the City of Hope.</li></ul>
Preferred qualifications:<ul><li>
Bachelor's degree.</li><li>
Familiarity with medical records, health information systems, or related health field.</li></ul>
Additional Information:<ul><li>
COH employees may apply for a transfer or promotion to job openings for which they meet the minimum qualifications if they meet the following criteria:</li><li>
Employed at COH in current role for at least 6 months, unless otherwise stipulated in an applicable collective bargaining agreement.</li><li>
Are in good standing and have no current performance issues.</li></ul>
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.
City of Hope is an equal opportunity employer.
To learn more about our Comprehensive Benefits, please CLICK HERE.</div></div>

Clinical Research Associate II

NYU Langone Health

<div>NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.
 
 
For more information, go to med.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, Twitter and Instagram.

Position Summary: 
We have an exciting opportunity to join our team as a Research Associate.
 
 
In this role, the successful candidate is responsible for conducting independent basic science experimentation based on research conducted in the assigned laboratory under the mentorship of a senior scientist. Individual is expected to seek to build a portfolio of research accomplishments in preparation for acquiring a higher degree in biomedical research or medicine.

Job Responsibilities:
<ul>
<li>After a period of time working in the laboratory, the candidate will be expected to train graduate students and post-doctoral fellows in experimental design, technique and performance.</li>
<li>Generates hypotheses and designs and performs experiments to test them.</li>
<li>Executes multiple experiments simultaneously over time independently.</li>
<li>Records all experimental findings in a laboratory notebook, analyze and interpret experimental findings.</li>
<li>Based on results, independently suggests and tests modifications to protocols.</li>
<li>Prepares figures and diagrams for presentations and publications.</li>
<li>Communicates results and collaborates with other professionals in the lab.</li>
<li>Demonstrates a significant level of intellectual input into the design of the project.</li>
<li>Presents findings at lab meeting, responds to challenges, and participates in exchanges of ideas to advance the science.</li>
<li>Reads and understands relevant scientific literature.</li>
<li>Contributes to the preparation of articles on research outcomes and progress and to the submission of same for publication.</li>
<li>Participates in the editing and proofing of grant proposals, annual grant reports, and manuscripts for publication and recommends modifications to the Principal Investigator.</li></ul> 


Minimum Qualifications: 
To qualify you must have a College graduate with a B.S. or B.A. in Biomedical or Physical Sciences. A minimum commitment of two years is required and placement in position may not exceed three years.

Preferred Qualifications: 
Prior research experience in a laboratory setting.

Qualified candidates must be able to effectively communicate with all levels of the organization.
 
 
NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents. At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package. Our offerings provide a robust support system for any stage of life, whether it's developing your career, starting a family, or saving for retirement. The support employees receive goes beyond a standard benefit offering, where employees have access to financial security benefits, a generous time-off program and employee resources groups for peer support. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Join us and experience the extensive resources and services designed to enhance your overall quality of life for you and your family.
 
 
NYU Grossman School of Medicine is an equal opportunity employer and committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. We require applications to be completed online.
 
 
View Know Your Rights: Workplace discrimination is illegal.

NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $47,033.89 - $50,000.00 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.

To view the Pay Transparency Notice, please click here</div>

Research Associate - Mazzoni Lab

The Emmes Company, LLC

<div>Overview:
<div>
Clinical Research Associate II 
 
Be Part of One Team, One Purpose. 
 
At Emmes Group, we&rsquo;re shaping the future of clinical research&mdash;where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we&rsquo;ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience. 
 
Through our two business units&mdash;Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions &mdash;we are modernizing clinical trials and accelerating the development of life-changing therapies. 
 
We believe that every clinical breakthrough starts with people&mdash;people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability. 
 
The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP.</div>
Responsibilities:
<ul><li>Under supervision of the project CRA staff oversight lead, example, Clinical Study Manager, Lead CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring visits such as qualification pre study visits, site initiation visits, interim routine monitoring visits, closeout visits, and for cause visits.</li><li>
As part of the site visits, independently conducts Informed Consent ICF review, source data verification source document review, review for compliance with required reporting tracking of adverse events and protocol deviations, investigator site file review, laboratory tour and specimen storage assessment, pharmacy Investigational Product IP Investigational Device ID storage location tour and storage condition assessment, IP ID accountability, facilities tours, and other activities per the site monitoring plan under minimal direction from the project CRA staff oversight lead.</li><li>
Documents observations and monitoring activities in a site visit report at the conclusion of the visit.</li><li>
Facilitates and oversees Action Item resolution post visit.</li><li>
Helps to ensure that clinical sites are conducting the study in compliance with protocol clinical investigational plan, SOPs, ICH GCP, and other applicable regulations.</li><li>
Provides training and retraining to site staff including protocol, GCP GDP, and other training under direction from the project CRA staff oversight lead.</li><li>
Identifies areas requiring follow up and improvement at each clinical study site and reports findings to project CRA staff oversight lead.</li><li>
Ensures all visits are conducted according to country regulations, ICH GCP, and company standard operating procedures</li><li>
Serves as point of contact for study site personnel to answer questions and resolve studyrelated issues under the direction of the project CRA staff oversight lead.</li><li>
May assist with the development and or review of study related materials including protocols, informed consent forms, monitoring plan, monitoring documents, etc.</li><li>
Prepares for and attends project team meetings and provides updates on project status and site specific performance</li><li>
Works collaboratively and effectively in a project team environment including internal and external colleagues to meet project objectives and timelines.</li><li>
Participates in Investigator Meetings or other client meetings as needed.</li><li>
Assists with filing and archiving of study documents.</li><li>
Assists in preparing sites for audits and may provide support and cooperation during audits inspections including translation to Auditor if needed.</li><li>
May assist with coordination of clinical study supplies.</li><li>
May assist with submission of applications notifications to Institutional Review Board IRB Ethics Committee EC Regulatory Authority.</li><li>
May assist with site recruitment oversight activities such as developing focused patient recruitment strategies and action plans.</li><li>
Performs site management activities as required</li><li>
Performs other duties as assigned</li><li>
Complies with all policies and standards</li></ul>
Qualifications:
<ul><li>Bachelor's Degree Scientific discipline preferred or equivalent work experience Required</li><li>
1-3 years 1-2 years of relevant monitoring experience (on-site and remote) Required</li><li>
Proficient with MS Office Suite High</li><li>
Excellent computer and organizational skills High</li><li>
High level of attention to detail required High</li><li>
Ability to work on varying projects and exercise critical thinking High</li><li>
self starter who can work remotely and a team player who can work cross functionally with some oversight High</li><li>
Knowledgeable in clinical research operations, including interpretation and implementation of country regulations and ICH guidelines, as required per their role as a CRA High</li><li>
Excellent organizational, interpersonal, and communication skills both oral and written High</li><li>
Demonstrated problem solving skills, self motivated, and adaptable to a dynamic environment High</li><li>
Knowledgeable in prioritization, problem solving, organization, critical thinking, decisionmaking, time management, and planning activities High</li><li>
Ability to collaborate with internal and external colleagues and work well in a team oriented setting High</li></ul><div></div><div> 
If you&rsquo;re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose. 
 
CONNECT WITH US! 
Find us on LinkedIn:/the-emmes-group/ 
Visit our website:https://www.theemmesgroup.com/</div></div>

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5581 research associate jobs Near Me

Research Associate

Research Associate

Laboratory Research Associate

Clinical Research Associate

Clinical Research Associate II

Research Associate - Mazzoni Lab

Clinical Research Associate II